进行性共济失调患者的症状负担及其对其亲友的广泛影响:一项横断面研究

AMRC open research Pub Date : 2021-11-30 eCollection Date: 2021-01-01 DOI:10.12688/amrcopenres.13036.1
Anja Lowit, Julie Greenfield, Emily Cutting, Ruby Wallis, Marios Hadjivassiliou
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引用次数: 0

摘要

背景:进行性共济失调是一种复杂的疾病,可导致多种症状。虽然我们目前对与各种类型的共济失调相关的症状模式有了相对较好的了解,以及这些疾病如何随着时间的推移而发展,但它们对共济失调患者的影响却知之甚少。此外,人们对护理人员、朋友和家人如何受到它们的影响知之甚少。本文旨在提供有关共济失调患者及其亲友的医学症状和日常挑战的存在和影响的初步信息。方法:数据摘自英国共济协会对其会员的调查。报告了366名共济失调患者和52名亲友的看法。分析了整个组的数据,以及样本中代表的三种最常见的共济失调类型,弗里德赖希共济失调,遗传性共济失调(不包括弗里德赖希共济失调)和原因不明的小脑性共济失调。结果:该调查证实了先前研究中描述的症状模式,但进一步表明,这些症状的影响可能因共济失调人群而异。在日常挑战中也观察到类似的结果。朋友和亲戚经历了与共济失调患者类似的挑战,这表明所提供的支持必须考虑到那些支持共济失调患者和患者的人。答复者还强调了在获得支助服务方面的限制,并不是所有的服务都能充分满足他们的具体需要。结论:本研究为进一步研究共济失调患者及其照顾者、朋友和亲戚的需求提供了信息。此类研究将支持治疗试验设计,确保考虑到患者的需求,帮助根据患者的需求量身定制支持服务,并确保卫生保健专业人员具备充分解决这些问题的必要技能。
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Symptom burden of people with progressive ataxia, and its wider impact on their friends and relatives: a cross-sectional study.

Background: Progressive ataxias are complex disorders that result in a wide variety of symptoms. Whilst we currently have a relatively good understanding of the symptom patterns associated with the various types of ataxia, and how these diseases progress over time, their impact on the person with ataxia is less well understood. In addition, little is known about how carers, friends and families are affected by them. This paper aims to provide preliminary information on the presence and impact of medical symptoms and day-to-day challenges on people with ataxia and their friends and relatives.

Method: Data were extracted from a survey by Ataxia UK for their members. The views of 366 people with ataxia and 52 friends and relatives are reported. Data were analysed for the entire groups, as well as for the three most common ataxia types represented in the sample, Friedreich's ataxia, inherited ataxia (excluding Friedreich's ataxia), and cerebellar ataxia of unknown cause.

Results: The survey confirmed the symptom patterns described in previous research, but further showed that the impact of these symptoms can vary across ataxia populations. Similar findings were observed for day-to-day challenges. Friends and relatives experienced similar challenges to people with ataxia, indicating that support provided has to consider those supporting people with ataxia as well as the patient. Respondents also highlighted limitations in terms of accessing support services, and not all services were able to cater fully to their specific needs.

Conclusion: This study begins to provide information that can be used in further research to explore the needs of people with ataxia and their carers, friends, and relatives. Such research will support treatment trial design, ensuring patients' needs are considered, help to tailor support services to their needs, and ensure health care professionals have the necessary skills to fully address them.

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